Muscular Dystrophy, Duchenne
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The purpose of this Position Stand is to provide guidance to professionals who counsel and prescribe individualized exercise to… Expand Duchenne muscular dystrophy (DMD) is a severe, progressive disease that affects 1 in 3600-6000 live male births. Although… Expand Optimum management of Duchenne muscular dystrophy (DMD) requires a multidisciplinary approach that focuses on anticipatory and… Expand Nitric oxide (NO) is synthesized in skeletal muscle by neuronal-type NO synthase (nNOS), which is localized to sarcolemma of fast… Expand ALTHOUGH murine X-linked muscular dystrophy (mdx) and Duchenne muscular dystrophy (DMD) are genetically homologous and both… Expand The mdx mouse is an X-linked myopathic mutant, an animal model for human Duchenne muscular dystrophy. In both mouse and man the… Expand The application of recombinant DNA technology to prenatal diagnosis of many recessively inherited X-linked diseases is… Expand A deficiency of the protein dystrophin has recently been shown to be the probable cause of Duchenne's muscular dystrophy. We… Expand The protein product of the human Duchenne muscular dystrophy locus (DMD) and its mouse homolog (mDMD) have been identified by… Expand The 14 kb human Duchenne muscular dystrophy (DMD) cDNA corresponding to a complete representation of the fetal skeletal muscle… Expand